NDC11 85938000650
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 85938-0006-50 | 85938-0006 |
| 85938-006-50 | 85938-006 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ICD Moisture Layer Sunscreen | HOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE | ICD Moisture Layer Sunscreen | 3a2a74f2-9fed-808f-e063-6294a90a410c | 2025-07-18 | Warnings | 85938-006-50 85938-006 85938000650 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.